A multifunctional dual cation doping strategy to stabilize high-voltage medium-nickel low-cobalt lithium layered oxide cathode.

High-voltage medium-nickel low-cobalt lithium layered oxide cathode materials are intriguing for lithium-ion batteries (LIBs) applications because of their relatively low cost and high capacity. Unfortunately, high charging voltage induces bulk layered structure decline and interface environment deterioration, low cobalt content reduces lithium diffusion kinetics, severely limiting the performance liberation of this kind of cathode. Here, a multifunctional Al/Zr dual cation doping strategy is employed to enhance the electrochemical performance of LiNiCoMnO (NCM) cathode at a high charging cut-off voltage of 4.

Antimony Nanoparticles Encapsulated in Self-Supported Organic Carbon with a Polymer Network for High-Performance Lithium-Ion Batteries Anode.

Antimony (Sb) demonstrates ascendant reactive activation with lithium ions thanks to its distinctive puckered layer structure. Compared with graphite, Sb can reach a considerable theoretical specific capacity of 660 mAh g by constituting LiSb safer reaction potential. Hereupon, with a self-supported organic carbon as a three-dimensional polymer network structure, Sb/carbon (3DPNS-Sb/C) composites were produced through a hydrothermal reaction channel followed by a heat disposal operation.

Gospel for Improving the Lithium Storage Performance of High-Voltage High-Nickel Low-Cobalt Layered Oxide Cathode Materials.

High-voltage high-nickel low-cobalt lithium layered oxide cathodes show great application prospects for lithium-ion batteries due to their low cost and high capacity. However, deterioration of the bulk structure and the electrode-electrolyte interface will significantly endanger the cycle life and thermal stability of the battery as the nickel content and voltage increase. We present here a lattice doping strategy to greatly improve the cell performance by doping a small dose of Ti (2 mol %) in LiNiCoMnO.

Unraveling the New Role of Metal-Organic Frameworks in Designing Silicon Hollow Nanocages for High-Energy Lithium-Ion Batteries.

Metal-organic framework (MOF)-derived materials are attracting considerable attention because of the moldability in compositions and structures, enabling greater performances in diverse applications. However, the nanostructural control of multicomponent MOF-based complexes remains challenging due to the complexity of reaction mechanisms. Herein, we present a surface-induced self-nucleation-growth mechanism for the zeolitic imidazolate framework (ZIF) to prepare a new type of ZIF-8@SiO polyhedral nanoparticles.

A highly promising high-nickel low-cobalt lithium layered oxide cathode material for high-performance lithium-ion batteries.

Reducing cobalt dependency has attracted great interest for lithium batteries manufacturing due to limited cobalt resources and high prices. A highly promising LiNiCoMnO (NCM60535) high-nickel low cobalt lithium layered oxide cathode material is successfully prepared by systematically examining the two key synthesis conditions of pH and annealing temperature. The obtained materials exhibit a uniform size distribution, good spherical morphology, clear structure, and homogeneous element distribution.

An SiO anode strengthened by the self-catalytic growth of carbon nanotubes.

Modification using carbon nanotubes (CNTs) is one of the most important strategies to boost the performance of materials in various applications, among which the CNT-modified silicon-based anodes have gained considerable attention in lithium-ion batteries (LIBs) due to their improved conductivity and cycle stability. However, the realization of a close-knit CNT coating on silicon (Si) through an efficient and cost-effective approach remains challenging. Herein, a new in situ self-catalytic method by acetylene treatment is presented, in which, CNTs can be directly grown and knitted on the SiO particles to construct a conductive additive-free SiO@CNT anode.

Insight into the Coprecipitation-Controlled Crystallization Reaction for Preparing Lithium-Layered Oxide Cathodes.

The nucleation and growth of spherical NiCoMn(OH) agglomerates using the hydroxide coprecipitation (HCP) method in the presence of ammonia is investigated through chemical equilibrium calculations and experiments. In the nucleation stage, the transition metal ions in the salt solution gradually complete the nucleation reaction in the diffusion process from pH 5.4 to 11 after dropping into the continuously stirred tank reactor, and then Me(NH) and Me(OH)(s) (Me: Ni, Co, and Mn) reach a dynamic precipitation dissolution equilibrium.

Enabling high electrochemical activity of a hollow SiO anode by decorating it with ultrafine cobalt nanoparticles and a carbon matrix for long-lifespan lithium ion batteries.

Silica is a very promising anode material for lithium-ion batteries, due to its advantages of being resource-rich and having high theoretical specific capacity. However, poor electrochemical activity severely limits its practical application. To solve this issue, a nanosheet-assembled silica hierarchical hollow sphere decorated with ultrafine cobalt nanoparticles and carbon (SiO2/Co/C) is successfully synthesized.